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CVD aluminide coatings deposited on a Directionally Solidified (DS) substrate were oxidized at 1,100°C up to 240 h under isothermal and cyclic oxidation conditions to study the growth mechanisms of the oxide scales and the possible degradation of the coatings. The specimens were investigated using light and scanning electron (SEM) microscopy, energy-dispersive spectrometry (EDS) and X-Ray Diffraction (XRD). The results indicate that the coatings provide a much greater beneficial effect under isothermal conditions than upon cycling. The cycled specimens undergo oxide-scale spallation and increased roughening, which can derive from growth and thermal stresses as well as from the NiAl ? Ni 3 Al phase transformation associated with Al depletion. Under isothermal conditions, typical oxide scales formed with the appearance of some rumples. However, the origin of rumpling is uncertain from these experimental results.

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In this work, superhydrophobic cerium oxide coating surface (111) with dual scale texture on Ni20Cr substrate is obtained by combination of electropolishing the substrate and subsequent cathodic electrodeposition and long-term UVH surface relaxation. To form hierarchical structures of CeO2 is controllable by varying the substrate roughness, and electropolishing period. The results indicated that at the optimal condition, the surface of the cerium oxide coating showed a superhydrophobicity with a great water contact angle (151.0 ± 1.4°) with Gecko state. An interface model for electropolishing of substrate surface in cerium nitrate medium is proposed. We expect that this facile process can be readily and widely adopted for the design of superhydrophobic coating on engineering materials.